Fit Firm and Fabulous is voluntarily recalling lots 05/02/2015 to 05/01/2017 of Ultimate Herbal Slimcap capsules, to the consumer level. FDA analysis has found the product to contain undeclared sibutramine. Sibutramine was a previously approved controlled substance that was removed from the U.S. market in October 2010 for safety reasons.
FDA takes several actions involving genetically engineered plants and animals for food
Based on sound science and a comprehensive review, the U.S. Food and Drug Administration (FDA) is taking several important steps today regarding food from genetically engineered (GE) plants and animals, including the first approval for a genetically engineered animal intended for food, AquAdvantage Salmon. The agency is also issuing two guidances for manufacturers who wish to voluntarily label their products as containing ingredients from GE or non-GE sources: a draft guidance on labeling foods derived from Atlantic salmon, and a final guidance on foods derived from GE plants.
FDA moves quickly to approve easy-to-use nasal spray to treat opioid overdose
Today the U.S. Food and Drug Administration approved Narcan nasal spray, the first FDA-approved nasal spray version of naloxone hydrochloride, a life-saving medication that can stop or reverse the effects of an opioid overdose. Opioids are a class of drugs that include prescription medications such as oxycodone, hydrocodone, and morphine, as well as the illegal drug heroin.
Wegmans Food Markets Issues Allergy Alert on Undeclared Tree Nuts (Cashews and Almonds) in Wegmans Italian Classics Butternut Squash Ravioli, 9 oz.
Wegmans Food Markets, Inc. is recalling Wegmans Italian Classics Butternut Squash Ravioli, 9 oz. (UPC #77890 36434), because the product may contain undeclared cashews and almonds. People who have an allergy or severe sensitivity to cashews or almonds run the risk of serious or life-threatening allergic reaction if they consume this product.
Ashdon Farms Issues Allergy Alert on Honey Mustard Pretzel Mix and Honey Mustard Mix
Ashdon Farms, Waukesha, WI 53188 is alerting consumers that Honey Mustard Pretzel Mix sold under the Girl Scouts of the USA brand and Honey Mustard Mix sold under the Ashdon Farms brand distributed to consumers on or before November 15, 2015 are being recalled because milk is not declared in the contains statement on the label.
FDA takes action to protect consumers from potentially dangerous dietary supplements
The U.S. Food and Drug Administration, in partnership with other government agencies, today announced the results of a yearlong sweep of dietary supplements to identify potentially unsafe or tainted supplements. The sweep resulted in civil injunctions and criminal actions against 117 various manufacturers and/or distributors of dietary supplements and tainted products falsely marketed as dietary supplements. Among the cases announced today is a criminal case charging USPlabs LLC and several of its corporate officers. USPlabs was known for its widely popular workout and weight loss supplements, which it sold under names such as Jack3d and OxyElite Pro.
CHS Inc. Issues Voluntary Recall of Certain Kountry Buffet and Provider Pellet Products Due to Excessive Copper
CHS Inc. announced today it has implemented a voluntary recall of 50-pound packages of its Kountry Buffet 14% Text and Provider 15% Pellet, both for Mature Cattle, Horses, Goats & Sheep due to excessive levels of copper. No illnesses or deaths have been reported to date.
FDA Orders Recall under Consent Decree for all Custom Ultrasonics Automated Endoscope Reprocessors
The U.S. Food and Drug Administration today ordered Custom Ultrasonics to recall all of its automated endoscope reprocessors (AERs) from health care facilities due to the firm’s continued violations of federal law and a consent decree entered with the company in 2007. The identified violations could result in an increased risk of infection transmission.
FDA approves Darzalex for patients with previously treated multiple myeloma
Today the U.S. Food and Drug Administration granted accelerated approval for Darzalex (daratumumab) to treat patients with multiple myeloma who have received at least three prior treatments. Darzalex is the first monoclonal antibody approved for treating multiple myeloma.
Virginia Diner, Inc. Issues Allergy Alert on Undeclared Peanut Allergen in Pecan Turtledoves Chocolate Caramel Pecan Clusters (Candy)
Virginia Diner, Inc. is voluntarily recalling, as a precaution, 10 oz. cans of Happy Holidays Pecan Turtledoves Chocolate Caramel Pecan Clusters (Candy) at the company’s Wakefield, VA location because they may contain peanuts and peanut allergens. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
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